Creatine transport and creatine kinase activity is required for CD8+ T cell immunity
A cell-intrinsic role for creatine transport and creatine transphosphorylation is demonstrated, independent of their effects on global cellular energy charge, in supporting CD8+ T cell homeostasis and effector function.
Abstract
The factors that promote T cell expansion are not fully known. Creatine is an abundant circulating metabolite that has recently been implicated in T cell function; however, its cell-autonomous role in immune-cell function is unknown. Here, we show that creatine supports cell-intrinsic CD8<sup>+</sup> T cell homeostasis. We further identify creatine kinase B (CKB) as the creatine kinase isoenzyme that supports these T cell properties. Loss of the creatine transporter (Slc6a8) or Ckb results in compromised CD8<sup>+</sup> T cell expansion in response to infection without influencing adenylate energy charge. Rather, loss of Slc6a8 or Ckb disrupts naive T cell homeostasis and weakens TCR-mediated activation of mechanistic target of rapamycin complex 1 (mTORC1) signaling required for CD8<sup>+</sup> T cell expansion. These data demonstrate a cell-intrinsic role for creatine transport and creatine transphosphorylation, independent of their effects on global cellular energy charge, in supporting CD8<sup>+</sup> T cell homeostasis and effector function.